AR059481A1 - Derivados de 1, 3-dihidro-imidazo[4, 5-c]piridin-2-ona como agonista del receptor tlr7, un metodo para su preparacion, intermediarios de sintesis de los mismos, una composicion farmaceutica que los comprende y su uso en la elaboracion de un medicamento para el tratamiento de infecciones viricas. - Google Patents

Derivados de 1, 3-dihidro-imidazo[4, 5-c]piridin-2-ona como agonista del receptor tlr7, un metodo para su preparacion, intermediarios de sintesis de los mismos, una composicion farmaceutica que los comprende y su uso en la elaboracion de un medicamento para el tratamiento de infecciones viricas.

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Publication number
AR059481A1
AR059481A1 ARP070100607A ARP070100607A AR059481A1 AR 059481 A1 AR059481 A1 AR 059481A1 AR P070100607 A ARP070100607 A AR P070100607A AR P070100607 A ARP070100607 A AR P070100607A AR 059481 A1 AR059481 A1 AR 059481A1
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AR
Argentina
Prior art keywords
alkyl
cycloalkyl
aryl
alkylene
heterocyclyl
Prior art date
Application number
ARP070100607A
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English (en)
Inventor
Peter Jones
Cameron David Pryde
Duc Tran Thien
Original Assignee
Pfizer Ltd
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Application filed by Pfizer Ltd filed Critical Pfizer Ltd
Publication of AR059481A1 publication Critical patent/AR059481A1/es

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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
    • C07D213/79—Acids; Esters
    • C07D213/80—Acids; Esters in position 3
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12—Antivirals
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12—Antivirals
    • A61P31/14—Antivirals for RNA viruses
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12—Antivirals
    • A61P31/20—Antivirals for DNA viruses
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12—Antivirals
    • A61P31/20—Antivirals for DNA viruses
    • A61P31/22—Antivirals for DNA viruses for herpes viruses
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D213/72—Nitrogen atoms
    • C07D213/75—Amino or imino radicals, acylated by carboxylic or carbonic acids, or by sulfur or nitrogen analogues thereof, e.g. carbamates
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04—Ortho-condensed systems

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Virology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Communicable Diseases (AREA)
  • Oncology (AREA)
  • Engineering & Computer Science (AREA)
  • Molecular Biology (AREA)
  • Biotechnology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)

Abstract

Derivados de 1,3-dihidro-imidazo[4,5-c]piridin-2-ona como modificadores de la respuesta inmune de formula (1), que actuan de forma selectiva por agonismo de receptores similares a ToII (TLR), a usos de los mismos, a procedimientos para la preparacion de los mismos, a intermedios usados en la preparacion de los mismos ya composiciones que contienen dichos inhibidores. Estos inhibidores tienen utilidad en una diversidad de áreas terapéuticas incluyendo el tratamiento de enfermedades infecciosas tales como hepatitis (por ejemplo, HCV, HBC), infecciones víricas genéticamente relacionadas y cáncer. Reivindicacion 1: Un compuesto de formula (1) o una sal o solvato farmacéuticamente aceptable de dicho compuesto o tautomero, en la que (a) Y es un enlace directo, y R3 se selecciona entre arilo, alquilo C1-6 y alquilen C1-4-O-alquilo C1-4; o (b) Y es alquileno C1-4, y R3 se selecciona entre arilo, cicloalquilo C3-7 y un heterociclilo de 3 a 10 miembros; Z es un oxigeno o está ausente; R1 se selecciona entre H, halogeno, OH, CN, alquilo C1-6, cicloalquilo C3-7, alcoxi C1-5, -NHSO2R6, -NR6R7, -C(O)R6, -CO2R6, -C(O)NR6R7, -C(O)NR6SO2R8, arilo y heterociclilo de 3 a 10 miembros; R2 se selecciona entre H, halogeno, OH, alquilo C1-6, cicloalquilo C3-7, alcoxi C1-6, -NR6R7, -CO2R6, -C(O)NR6R7, -C(O)NR6SO2R8,y heterociclilo de 3 a 10 miembros; o R1 y R2 pueden unirse para formar una union de tipo alquileno C2-5, incorporando dicha union opcionalmente 1 o 2 heteroátomos seleccionados cada uno de ellos independientemente entre N, O y S; R5 está ausente y R4 se selecciona entre H, cicloalquilo C3-7, arilo, (CH2)arilo, -C(O)R9, -CO2R9, -alquilen C1-6-O-C(O)R9, -alquilen C1-6-O-CO2R9, -C(O)NR9R10, - alquilen C1-6-O-C(O)NR9R10 y -alquilen C1-6-O-P(O)(OH)2; o R4 está ausente y R5 se selecciona entre R9, -C(O)R9, -CO2R9, -alquilen C1-6-O-C(O)R9, -alquilen C1-6-O-CO2R9, -C(O)NR9R10, -alquilen C1-6-O-C(O)NR9R10 y -alquilen C1-6-O-P(O)(OH)2, cada uno de R6 y R7 se selecciona independientemente entre H, alquilo C1-6, cicloalquilo C3-7, y -alquilen C1-6-cicloalquilo C3-7; o R6 y R7 tomados junto con el nitrogeno al que están unidos forman un heterociclo saturado de 3 a 6 miembros que contiene opcionalmente uno o dos heteroátomos adicionales seleccionados entre N, O y S; R8 se selecciona entre alquilo C1-6, cicloalquilo C3-7 y fenilo; cada uno de R9 y R10 se selecciona independientemente entre H, alquilo C1-6, cicloalquilo C3-7, arilo, - (CH2)arilo y heterociclilo de 3 a 10 miembros; o R9 y R10, tomados junto con el nitrogeno al que están unidos, forman un grupo heterociclilo de 3 a 10 miembros; R11 y R12 se seleccionan independientemente entre H y alquilo C1-6; o R11 y R12 junto con el N al que están unidos forman un heterociclilo saturado de 3 a 6 miembros que contiene opcionalmente uno o dos heteroátomos adicionales seleccionados entre N, O y S; estando dichos grupos alquilo, cicloalquilo, alcoxi, arilo y heterociclilo opcionalmente sustituidos con uno o más átomos o grupos seleccionados independientemente entre halogeno, OH, oxo, CF3, CN, alquilo C1-6, cicloalquilo C3-7, alcoxi C1-6, -alquileno C1-6-O-alquilo C1-6, -alquilen C1-6-OH, NR11R12, -alquilen C1-6- NR11R12, arilo y heterociclilo de 3 a 10 miembros; con la condicion de que cuando R1 y R2 son H, y Z y R5 están ausentes, entonces (a) R4 no es metilo cuando Y-R3 es etilo; y (b) R4 no es H o metilo cuando Y-R3 es metilo.
ARP070100607A 2006-02-17 2007-02-13 Derivados de 1, 3-dihidro-imidazo[4, 5-c]piridin-2-ona como agonista del receptor tlr7, un metodo para su preparacion, intermediarios de sintesis de los mismos, una composicion farmaceutica que los comprende y su uso en la elaboracion de un medicamento para el tratamiento de infecciones viricas. AR059481A1 (es)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US77458006P 2006-02-17 2006-02-17
US82973006P 2006-10-17 2006-10-17
US87002006P 2006-12-14 2006-12-14

Publications (1)

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AR059481A1 true AR059481A1 (es) 2008-04-09

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ARP070100607A AR059481A1 (es) 2006-02-17 2007-02-13 Derivados de 1, 3-dihidro-imidazo[4, 5-c]piridin-2-ona como agonista del receptor tlr7, un metodo para su preparacion, intermediarios de sintesis de los mismos, una composicion farmaceutica que los comprende y su uso en la elaboracion de un medicamento para el tratamiento de infecciones viricas.

Country Status (17)

Country Link
US (1) US7691877B2 (es)
EP (1) EP1987030B1 (es)
JP (1) JP2009528989A (es)
KR (1) KR20080085232A (es)
AR (1) AR059481A1 (es)
AT (1) ATE532784T1 (es)
AU (1) AU2007216247A1 (es)
BR (1) BRPI0707945A2 (es)
CA (1) CA2640672A1 (es)
ES (1) ES2374455T3 (es)
IL (1) IL193173A0 (es)
MX (1) MX2008010611A (es)
NL (1) NL2000480C2 (es)
PE (1) PE20070983A1 (es)
TW (1) TW200800995A (es)
UY (1) UY30169A1 (es)
WO (1) WO2007093901A1 (es)

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